Effect of oils sources on blood lipid parameters of commercial laying hens

Effect of oils sources on blood lipid parameters of commercial laying hens

Murata LS^{* I}; Ariki J^II; Machado CR^III; Silva L da PG da^IV; Rezende MJM^I

^IDocente da Faculdade de Agronomia e Medicina Veterinária da UnB – Brasília/DF

^IIDocente do Departamento de Zootecnia de Não Ruminantes da FCAV/UNESP – Jaboticabal/SP

^IIIDocente do Departamento de Morfologia e Fisiologia Animal da FCAV/UNESP

^IVDocente do Departamento de Zootecnia da UFPB – Areia/PB

^{Correspondence}

ABSTRACT

The experiment was carried out to verify if total cholesterol, HDL-cholesterol and triacylglicerol plasma levels are affected when laying hens are fed rations containing different dietary oil sources. One hundred sixty 50 week-old hens, assigned to four treatments with five replicates using 8 hens per replicate were used. The experimental period was of 84 days divided in 3 cycles of 28 days each. In the last day of each cycle, blood samples of 2 hens per replicate were randomly choose and blood samples were collected. On the other hand, blood was also collected at 7 am, 11 am and 3 pm aiming to study the daily changes of these lipids. Blood lipid parameters were not affected by different dietary oil sources (p > 0.05); however, HDL-cholesterol did change during the day, giving evidence that this lipid is indeed involved in the egg yolk formation.

Keywords: Blood lipids, diet, laying hens, oil source.

INTRODUCTION

The search of new procedures to improve the quality of foods of animal origin is an unquestionable tendency in animal production. One of the relevant subjects, in this context, is the attempt to improve the quality of the egg yolk lipids content profile of commercial laying hens for human consumption.

Egg is constituted mainly by water, which correspond, approximately, to 75% of the total egg weight. However, chemical components of the egg are not uniformly distributed between the yolk and albumen, with the albumen volume being twice of the yolk. Although both fractions contain similar amount of proteins, carbohydrates, and minerals, the yolk contains all lipids of the egg (Romanoff & Romanoff, 1963).

Nutrition, genetic and pharmacological agents can affect cholesterol deposition in the egg yolk (Hargis, 1988). Concerning nutrition, one of the methods developed to change the lipid profile of eggs has been the use of oil types rich in fatty acids (Leaf & Weber, 1988), commonly used as a source of energy in the diets of laying hens.

Connor et al. (1965) demonstrated that laying hens transfer blood cholesterol for yolk development and has been constituted in the principal mechanism of cholesterol excretion (Naber, 1976), followed by bile excretion (Hargis, 1988).

The organ where most of the lipogenesis takes place in poultry is the liver. Considering the ingredients of a ration, especially vegetables, cholesterol free, all lipid fractions deposited in the yolk are synthesized in the liver, which are afterwards sent through blood stream to different tissues of the body.

The results in the literature regarding the effect of dietary fatty acids intake on egg and plasma cholesterol concentrations are contradictory. Hollands et al., (1980) and Mori et al., (1999) verified that polyunsaturated fatty acids of dietetic oils decrease both the egg and the plasma cholesterol concentrations. On the other hand, Bartov et al. (1971) and Washburn & Nix (1974) did not observe such effect.

Oils have commonly been used as energy sources in diets for laying hens. Some of these oil sources are rich in elements such as long chain polyunsaturated fatty acid that can change the proportion of the constituents of the egg yolk.

The aim of this experiment was to verify the plasma levels of total cholesterol (mg/dL), HDL-cholesterol (mg/dL), and triacylglicerol (mg/dL) in laying hens blood, fed diets containing different oil sources.

MATERIAL AND METHODS

Fifty week-old Lohmann White laying hens were used. These hens were fed diets containing soy, fish, canola and poultry by-product oils at the 3% level and soy oil was used as the control, following the recommendations of NRC (1994) (Table 1). Experimental diets and water were provided for ad libitum consumption. Table 2 shows the fatty acids composition of each oil source.

One hundred and sixty hens were distributed in a random experimental design with 4 treatments (oil source - soy, canola, fish and poultry by-product) and 5 replicates of 8 birds each. The general management of hens followed the strain recommendations (Manual de criação e manejo, 1996).

The experimental period was 84 days divided in three cycles of 28 days each. A total of 3 mL of blood drawn by cardiac puncture was collected from the same hen at 7:00am, 11:00am and 3:00pm on the last day of each cycle, being two hens per replicate choose at random.

Plasma was obtained by blood centrifugation and total cholesterol, HDL-cholesterol and triacylglicerol were determined using commercial kits (LabTest Diagnosis).

The data were submitted to analysis of variance according to Banzatto & Kronka (1992) using the software "Sistema de Análise Estatística". The means were compared using the test of Tukey at 5% probability.

RESULTS AND DISCUSSION

The means plasma total cholesterol, HDL-cholesterol and triacylglicerol, as well as egg yolk total cholesterol contents obtained at the end of each laying cycle are shown in Table 3. Plasma values were not affected (p > 0.05) by dietary treatments, indicating to be a singular characteristic of the laying hens, as pointed out by Chapman (1980). Previous reports had indicated that plasma cholesterol concentration is not related to egg yolk lipid level, although synthesized in the liver and transported by the blood (Sutton et al., 1984; Mendonça Jr., 1996). However, total cholesterol of egg yolk was affected by dietary oil source (p < 0.05) with lower values verified when soy oil was added to the ration.

Beyer & Jensen (1991) reported that the level of plasma cholesterol shows great variation suggesting that this effect could represents the synthesis and excretion of cholesterol through the liver, associated with the feed consumption or the ovulation period of the hen. A possible explanation for not being a clear relation between the blood cholesterol and the yolk cholesterol may lie on the fact that the available blood cholesterol for the growing oocyte rapidly varies in relation to time.

Plasma levels of triacylglicerol and total cholesterol did not differ (p > 0.05) during the day, but plasma HDL-cholesterol levels was different (p < 0.05) (Table 4). The lowest plasma level of HDL-cholesterol was obtained at 11:00 am. According to Chobanian & Hollander (1962), this difference could be due to the observation that HDL-cholesterol belong to the "fast turnover cholesterol pool"; and yet, it can still be related to the interval between egg production, considering that 80% of hens lay eggs in the morning.

CONCLUSION

Feeding diets containing different oil sources (soy, fish, canola and poultry by-product oils) at 3%, has no effect on plasma total cholesterol, HDL-cholesterol and triacylglicerol levels of laying hens plasma, but plasma level of HDL-cholesterol seems to be related with egg formation cycle.

Acknowledgments

We wish to thank COCAMAR, Granja Mizumoto, and Granja Sertanejo for providing the oils used in this research.

Arrived: november/02

Approved: september/03

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Publication Dates

• Publication in this collection
  13 Apr 2004
• Date of issue
  Dec 2003

History

• Accepted
  Sept 2003
• Received
  Nov 2002